KR970022547A - Chemically Amplified Forged Resist Compositions - Google Patents

Chemically Amplified Forged Resist Compositions Download PDF

Info

Publication number
KR970022547A
KR970022547A KR1019960044682A KR19960044682A KR970022547A KR 970022547 A KR970022547 A KR 970022547A KR 1019960044682 A KR1019960044682 A KR 1019960044682A KR 19960044682 A KR19960044682 A KR 19960044682A KR 970022547 A KR970022547 A KR 970022547A
Authority
KR
South Korea
Prior art keywords
group
compound
resist composition
carbon atoms
phenolic hydroxyl
Prior art date
Application number
KR1019960044682A
Other languages
Korean (ko)
Other versions
KR100231242B1 (en
Inventor
사토시 와타나베
오사무 와타나베
시게히로 나구라
도시노부 이시하라
Original Assignee
가나가와 지히로
신에츠 가가쿠 고교 가부시키가이샤
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 가나가와 지히로, 신에츠 가가쿠 고교 가부시키가이샤 filed Critical 가나가와 지히로
Publication of KR970022547A publication Critical patent/KR970022547A/en
Application granted granted Critical
Publication of KR100231242B1 publication Critical patent/KR100231242B1/en

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/039Macromolecular compounds which are photodegradable, e.g. positive electron resists
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/0045Photosensitive materials with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/1053Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
    • Y10S430/1055Radiation sensitive composition or product or process of making
    • Y10S430/106Binder containing

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Materials For Photolithography (AREA)

Abstract

본 화학증폭 포지형 레지스트 조성물은(A) 유기용매, (B) 베이스 수지, (C) 광산 발생제 및 임의로 (D) 용해속도조절제를 함유한다. 베이스 수지(B)는 서로 다른 산불안정기를 가지며 Mw가 3,000-300,000인 히드록시스티렌 공중합체이다.The chemically amplified forged resist composition contains (A) an organic solvent, (B) a base resin, (C) a photoacid generator, and optionally (D) a dissolution rate regulator. The base resin (B) is a hydroxystyrene copolymer having different acid labile groups and Mw of 3,000-300,000.

본 레지스트 조성물은 원자외선, 전자선 및 X선과 같은 화학방사선에 대한 감도가 높으며 수성 염기로 현상하여 패턴을 형성할 수 있고 따라서 미세 패터닝 기법에 사용하기에 적합하다.The resist composition is highly sensitive to actinic radiation, such as far ultraviolet rays, electron beams and X-rays, and can be developed with aqueous bases to form patterns and thus suitable for use in fine patterning techniques.

Description

화학증폭 포지형 레지스트 조성물Chemically Amplified Forged Resist Compositions

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

제1도는 합성예 4에서 얻어진 중합체의 GPC 용출곡선을 나타내는 그래프이다.1 is a graph showing the GPC elution curve of the polymer obtained in Synthesis Example 4. FIG.

Claims (12)

(A) 유기용매, (B) 다음 일반식(1)의 반복단위를 갖고 중량평균분자량이 3,000 내지 300,000인 중합체형태의 베이스 수지(A) an organic solvent, (B) a base resin in the form of a polymer having a repeating unit of the following general formula (1) and having a weight average molecular weight of 3,000 to 300,000 (식에서 R1은 수소원자 또는 메틸기이고, R2및 R3는 서로 다른 산불안정기이고, p, q 및 r은 0.02p/(p+q+r)0.5, 0.01q/(p+q+r)0.3, 0(p+q)/(p+q+r)0.8을 만족시키는 양수이고, a는 1 내지 3의 양수이다), 및 (C) 광산발생제로 이루어지는 것을 특징으로 하는 화학증폭 포지형 레지스트 조성물.Wherein R 1 is a hydrogen atom or a methyl group, R 2 and R 3 are different acid labile groups, and p, q and r are 0.02 p / (p + q + r) 0.5, 0.01 q / (p + q + r) 0.3, 0 (p + q) / (p + q + r) A positive number satisfying 0.8, a is a positive number of 1 to 3), and (C) a chemically amplified forged resist composition comprising a photoacid generator. 제1항에 있어서, (D) 용해속도조절제를 더 포함하는 것을 특징으로 하는 레지스트 조성물.The resist composition of claim 1, further comprising (D) a dissolution rate adjusting agent. 제2항에 있어서, 용해속도조절제(D)가 중량평균분자량이 100 내지 1,000이며 분자내에 적어도 두 개의 페놀성 히드록실기를 갖는 화합물로서, 페놀성 히드록실기의 주소원자가 산불안정기에 의해 10% 내지 100%의 전체 평균 비율로 치환된 화합물인 것을 특징으로 하는 레지스트 조성물.The compound according to claim 2, wherein the dissolution rate controlling agent (D) is a compound having a weight average molecular weight of 100 to 1,000 and having at least two phenolic hydroxyl groups in a molecule, wherein the address atom of the phenolic hydroxyl group is 10% by an acid labile group. A resist composition, characterized in that the compound substituted in the total average ratio of 100%. 제2항에 있어서, 용해속도조절제(D)가 중량평균분자량이 1,000 초과 내지 3,000이며 분자내에 페놀성 히드록실기를 갖는 화합물로서, 페놀성 히드록실기의 수소원자가 산불안정기에 의해 0% 초과 내지 60%의 전체평균 비율로 부분치환된 화합물인 것을 특징으로 하는 레지스트 조성물.The compound according to claim 2, wherein the dissolution rate adjusting agent (D) is a compound having a weight average molecular weight of more than 1,000 to 3,000 and a phenolic hydroxyl group in the molecule, wherein the hydrogen atom of the phenolic hydroxyl group is more than 0% by an acid labile group. A resist composition, which is a compound partially substituted at a total average ratio of 60%. 제2항에 있어서, 용해속도조절제(D)가 (D-1) 중량평균분자량이 100 내지 1,000이며 분자내에 적어도 두개의 페놀성 히드록실기를 갖는 화합물로서, 페놀성 히드록실기의 수소원자가 산불안정기에 의해 10% 내지 100%의 전체 평균 비율로 치환된 화합물과 (D-2) 중량평균분자량이 1,000 초과 내지 3,000이며 분자내에 페놀성 히드록실기를 갖는 화합물로서 페놀성 히드록실기의 수소원자가 산불안정기에 의해 0% 초과 내지 60%의 전체 평균 비율로 부분치환된 화합물의 혼합물인 것을 특징으로 하는 레지스트 조성물.The compound according to claim 2, wherein the dissolution rate controlling agent (D) is a compound having a weight average molecular weight of (D-1) of 100 to 1,000 and having at least two phenolic hydroxyl groups in a molecule, wherein the hydrogen atom of the phenolic hydroxyl group is a wildfire. A compound substituted with a total average ratio of 10% to 100% by a ballast group, and (D-2) a compound having a weight average molecular weight of more than 1,000 to 3,000 and having a phenolic hydroxyl group in a molecule, wherein the hydrogen atom of the phenolic hydroxyl group is A resist composition, characterized in that it is a mixture of compounds partially substituted by an acid labile group at an overall average ratio of greater than 0% to 60%. 제3항 또는 제5항에 있어서, 중량평균분자량이 100 내지 1,000이며 분자내에 적어도 두개의 페놀성 히드록실기를 갖는 화합물이 다음 일반식(6) 내지(16)의 화합물중에서 선택된 적어도 한가지 화합물인 것을 특징으로 하는 레지스트 조성물.The compound according to claim 3 or 5, wherein the compound having a weight average molecular weight of 100 to 1,000 and having at least two phenolic hydroxyl groups in a molecule is at least one compound selected from compounds of the following general formulas (6) to (16): Resist composition, characterized in that. 식에서 R13및 R13은 수소 및 탄소원자수 1 내지 8의 직쇄상 또는 분지상 알킬 및 알켄일기로 구성된 군에서 독립적으로 선택되고, R14는 수소, 탄소원자수 1 내지 8의 직쇄상 또는 분자상 알킬 및 알켄일기, 및(R18)s-COOH로 구성된 군에서 선택되고, R15는 -(CH2)t-기(여기서 t는 2 내지 10이다), 탄소원자수 6 내지 10의 아릴렌기, 카르보닐기, 술포닐기, 산소원자 및 황원자로 구성된 군에서 선택되고, R16은 탄소원자수 1 내지 10의 알킬렌기, 탄소원자수 6 내지 10의 아릴렌기, 카르보닐기, 술포닐기, 산소원자 및 황원자로 구성된 군에서 선택되고, R17은 수소원자, 탄소원자수 1 내지 8의 직쇄상 또는 분자상 알킬기, 알켄일기, 히드록실-치환페닐 및 나프틸기로 구성된 군에서 선택되고, R18은 탄소원자수 1 내지 10의 직쇄상 또는 분자상 알킬렌기이고, k는(0) 내지 5의 정수이고, s는 0 또는 1이고, m, n, m′, n′, m″및 n″는 적어도 한개의 히드록실기가 각 페닐 골격에 결합되도록 m+n=8, m′+n′=5 및 m″+n″=4를 만족시키는 수이고, α는 식(13) 또는(14)의 화합물이 100 내지 1,000의 분자량을 가질 수 있는 수이다.Wherein R 13 and R 13 are independently selected from the group consisting of hydrogen and linear or branched alkyl of 1 to 8 carbon atoms and alkenyl group, R 14 is hydrogen, linear or molecular alkyl of 1 to 8 carbon atoms And an alkenyl group, and (R 18 ) s -COOH, wherein R 15 is a-(CH 2 ) t -group where t is 2 to 10 carbon atoms, an arylene group having 6 to 10 carbon atoms, and a carbonyl group , Sulfonyl group, oxygen atom and sulfur atom, R 16 is selected from the group consisting of alkyl group of 1 to 10 carbon atoms, arylene group of 6 to 10 carbon atoms, carbonyl group, sulfonyl group, oxygen atom and sulfur atom R 17 is selected from the group consisting of a hydrogen atom, a linear or molecular alkyl group having 1 to 8 carbon atoms, an alkenyl group, a hydroxyl-substituted phenyl, and a naphthyl group, and R 18 is a straight chain having 1 to 10 carbon atoms Or a molecular alkylene group, k is (0 ) Is an integer of 5 to 5, s is 0 or 1, and m, n, m ', n', m "and n" are m + n = 8, m so that at least one hydroxyl group is bonded to each phenyl skeleton. Is a number satisfying '+ n' = 5 and m ″ + n ″ = 4, and α is a number such that the compound of formula (13) or (14) may have a molecular weight of 100 to 1,000. 제4항 또는 제5항에 있어서, 중량평균분자량이 1,000 초과 내지 3,000이며 분자내에 페놀성 히드록실기를 갖는 화합물이 다음 일반식(17)의 반복 단위를 갖는 화합물중에서 선택된 적어도 한가지 화합물인 것을 특징으로 하는 레지스트 조성물.The compound according to claim 4 or 5, wherein the compound having a weight average molecular weight greater than 1,000 to 3,000 and having a phenolic hydroxyl group in the molecule is at least one compound selected from compounds having a repeating unit of the following general formula (17): Resist composition to be. 식에서 R은 산불안정기이고, c 및 d는 0c/(c+d)0.6을 만족시키는 수이다.Where R is an acid labile, c and d are 0 c / (c + d) A number satisfying 0.6. 제1항에 있어서, 식(1)에서 R2가 다음 일반식(2)The compound of claim 1, wherein in formula (1), R 2 is (식에서 R4및 R5는 수소원자 및 탄소원자수 1 내지 6의 직쇄상 또는 분지상 알킬기로 구성된 군에서 독립적으로 선택되고, R6는 탄소원자수 1 내지 10의 직쇄상, 분지상 또는 환상 알킬기이다)의 기이고, R3가 다음 일반식(3)Wherein R 4 and R 5 are independently selected from the group consisting of a hydrogen atom and a straight or branched alkyl group having 1 to 6 carbon atoms, and R 6 is a straight, branched or cyclic alkyl group having 1 to 10 carbon atoms ) And R 3 is the following general formula (3) (식에서 R7은 탄소원자수 1 내지 6의 직쇄상 또는 분지상 알킬기이고, b는 0 또는 1이다)의 기, 테트라히드로피란일기, 테트리히드로푸란일기 및 트리알킬실일기로 구성된 군에서 선택되는 것을 특징으로 하는 레지스트 조성물.Wherein R 7 is a straight or branched alkyl group having 1 to 6 carbon atoms, b is 0 or 1, and selected from the group consisting of a tetrahydropyranyl group, a tetrahydrofuranyl group and a trialkylsilyl group Resist composition, characterized in that. 제8항에 있어서, R2가 알콕시알킬기이고 R3가 tert-부톡시카르보닐기인 것을 특징으로 하는 레지스트 조성물.9. The resist composition of claim 8, wherein R 2 is an alkoxyalkyl group and R 3 is a tert-butoxycarbonyl group. 제1항에 있어서, (E) 염기성 화합물을 첨가제로서 더 포함하는 것을 특징으로 하는 레지스트 조성물.The resist composition according to claim 1, further comprising (E) a basic compound as an additive. 제1항에 있어서, 베이스 수지(B)가 1.0 내지 1.5의 분포를 갖는 단분산성 중합체인 것을 특징으로 하는 레지스트 조성물.The resist composition according to claim 1, wherein the base resin (B) is a monodisperse polymer having a distribution of 1.0 to 1.5. 제1항에 있어서, 광산발생제(C)가 오늄염인 것을 특징으로 하는 레지스트 조성물.The resist composition according to claim 1, wherein the photoacid generator (C) is an onium salt. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019960044682A 1995-10-09 1996-10-09 Chemically amplified positive resist composition KR100231242B1 (en)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
JP95-287944 1995-10-09
JP95-287945 1995-10-09
JP28794595 1995-10-09
JP28794495 1995-10-09
JP33790195 1995-12-01
JP95-337900 1995-12-01
JP33790095 1995-12-01
JP95-337901 1995-12-01

Publications (2)

Publication Number Publication Date
KR970022547A true KR970022547A (en) 1997-05-30
KR100231242B1 KR100231242B1 (en) 1999-11-15

Family

ID=27479469

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019960044682A KR100231242B1 (en) 1995-10-09 1996-10-09 Chemically amplified positive resist composition

Country Status (3)

Country Link
US (1) US6106993A (en)
KR (1) KR100231242B1 (en)
TW (1) TW448344B (en)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5942367A (en) * 1996-04-24 1999-08-24 Shin-Etsu Chemical Co., Ltd. Chemically amplified positive resist composition, pattern forming method, and method for preparing polymer having a crosslinking group
JP3823449B2 (en) * 1997-06-16 2006-09-20 住友化学株式会社 Photoresist composition
JP3875280B2 (en) * 1997-07-15 2007-01-31 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Improved dissolution inhibiting resist for microlithography
JP3353292B2 (en) * 1999-03-29 2002-12-03 日本電気株式会社 Chemically amplified resist
US6723483B1 (en) 1999-12-27 2004-04-20 Wako Pure Chemical Industries, Ltd. Sulfonium salt compounds
KR100553263B1 (en) * 2000-04-14 2006-02-20 주식회사 동진쎄미켐 Polymer for chemically amplified resist and resists using this polymer
JP3802732B2 (en) * 2000-05-12 2006-07-26 信越化学工業株式会社 Resist material and pattern forming method
JP3355175B2 (en) * 2000-05-16 2002-12-09 ティーディーケイ株式会社 Frame plating method and method of forming magnetic pole of thin film magnetic head
US6534239B2 (en) 2001-04-27 2003-03-18 International Business Machines Corporation Resist compositions with polymers having pendant groups containing plural acid labile moieties
KR100790418B1 (en) * 2001-06-22 2008-01-02 와코 쥰야꾸 고교 가부시키가이샤 Resist compositions
JP4025074B2 (en) * 2001-09-19 2007-12-19 富士フイルム株式会社 Positive resist composition
DE10147954B4 (en) * 2001-09-28 2007-04-19 Infineon Technologies Ag CARL for Bioelectronics: Substrate connection via conductive layer
DE10147953B4 (en) * 2001-09-28 2007-06-06 Infineon Technologies Ag CARL for Bioelectronics: Substrate connection via insulating layer
JP4595275B2 (en) * 2001-09-28 2010-12-08 住友化学株式会社 Chemically amplified positive resist composition
KR100465448B1 (en) * 2002-03-15 2005-01-13 제일모직주식회사 Photoresist composition
JP4189951B2 (en) * 2002-10-31 2008-12-03 東京応化工業株式会社 Chemically amplified positive resist composition
KR100900173B1 (en) 2004-02-20 2009-06-02 도오꾜오까고오교 가부시끼가이샤 Base material for pattern forming material, positive resist composition and method of resist pattern formation
JP3946715B2 (en) 2004-07-28 2007-07-18 東京応化工業株式会社 Positive resist composition and resist pattern forming method
JP4468119B2 (en) 2004-09-08 2010-05-26 東京応化工業株式会社 Resist composition and resist pattern forming method
JP4837323B2 (en) * 2004-10-29 2011-12-14 東京応化工業株式会社 Resist composition, resist pattern forming method and compound
WO2006059569A1 (en) 2004-12-03 2006-06-08 Tokyo Ohka Kogyo Co., Ltd. Positive resist composition and method of forming resist pattern
US7981588B2 (en) 2005-02-02 2011-07-19 Tokyo Ohka Kogyo Co., Ltd. Negative resist composition and method of forming resist pattern
JP4397834B2 (en) 2005-02-25 2010-01-13 東京応化工業株式会社 Positive resist composition, resist pattern forming method and compound
JP5138157B2 (en) 2005-05-17 2013-02-06 東京応化工業株式会社 Positive resist composition and resist pattern forming method
JP4813103B2 (en) 2005-06-17 2011-11-09 東京応化工業株式会社 COMPOUND, POSITIVE RESIST COMPOSITION AND METHOD FOR FORMING RESIST PATTERN
JP4732038B2 (en) 2005-07-05 2011-07-27 東京応化工業株式会社 COMPOUND, POSITIVE RESIST COMPOSITION AND METHOD FOR FORMING RESIST PATTERN
US7776510B2 (en) * 2007-06-13 2010-08-17 Tokyo Ohka Kogyo Co., Ltd. Resist composition, method of forming resist pattern, compound and acid generator
JP5039492B2 (en) * 2007-09-28 2012-10-03 富士フイルム株式会社 Positive resist composition and pattern forming method using the same
JP5039493B2 (en) * 2007-09-28 2012-10-03 富士フイルム株式会社 Positive resist composition and pattern forming method using the same
KR102456204B1 (en) * 2017-01-25 2022-10-18 도오꾜오까고오교 가부시끼가이샤 Resist composition and method of forming resist pattern
JP6986880B2 (en) 2017-07-12 2021-12-22 東京応化工業株式会社 Resist composition and resist pattern forming method

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69125634T2 (en) * 1990-01-30 1998-01-02 Wako Pure Chem Ind Ltd Chemically reinforced photoresist material
US5352564A (en) * 1993-01-19 1994-10-04 Shin-Etsu Chemical Co., Ltd. Resist compositions
JP3297199B2 (en) * 1993-09-14 2002-07-02 株式会社東芝 Resist composition
US5558971A (en) * 1994-09-02 1996-09-24 Wako Pure Chemical Industries, Ltd. Resist material
JP3198915B2 (en) * 1996-04-02 2001-08-13 信越化学工業株式会社 Chemically amplified positive resist material

Also Published As

Publication number Publication date
KR100231242B1 (en) 1999-11-15
US6106993A (en) 2000-08-22
TW448344B (en) 2001-08-01

Similar Documents

Publication Publication Date Title
KR970022547A (en) Chemically Amplified Forged Resist Compositions
KR940018702A (en) Resist composition
KR970071134A (en) Chemically amplified forged resist materials
KR970071135A (en) Chemically amplified forged resist materials
KR920013027A (en) Photosensitive composition
KR970028825A (en) New Sulfonium Salts and Chemically Amplified Forged Resist Materials
KR960008428A (en) Chemically Amplified Radiation-Sensitive Compositions
KR970007489A (en) Chemically amplified positive resist material
KR880014417A (en) Blocked monomers and polymers thereof for use as photoresist
KR920020276A (en) Pattern forming resist
KR960024676A (en) Positive resist composition
KR960038481A (en) Polymer compounds and chemically amplified positive resist materials
KR980002109A (en) Photosensitive polyimide precursor composition, and pattern formation method using the same
KR970066718A (en) Radiation-sensitive resin composition
KR960038480A (en) The chemically amplified positive resist composition
JP4411042B2 (en) Positive resist composition and pattern forming method using the same
KR960024672A (en) Chemically Amplified Forged Resist Compositions
KR950032084A (en) Sulfonium Salt and Chemically Amplified Forged Resist Compositions
JP4612999B2 (en) Positive resist composition and pattern forming method using the same
JP2004310004A5 (en)
KR970002470A (en) Positive Photoresist Composition
JP2002169295A5 (en)
KR980003839A (en) Chemically amplified forged resist materials
KR970071129A (en) Di or triphenylmonoterpene hydrocarbon derivatives, dissolution control agents and chemically amplified forged resist materials
KR960042219A (en) Si-containing polymer compound and photosensitive resin composition

Legal Events

Date Code Title Description
A201 Request for examination
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
O035 Opposition [patent]: request for opposition
O132 Decision on opposition [patent]
G171 Publication of modified document after post-grant opposition [patent]
O074 Maintenance of registration after opposition [patent]: final registration of opposition
FPAY Annual fee payment

Payment date: 20130801

Year of fee payment: 15

FPAY Annual fee payment

Payment date: 20140808

Year of fee payment: 16

LAPS Lapse due to unpaid annual fee